A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv698960



Internal ID15435612
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:112370167..112398862hg38UCSC Ensembl
InnerchrX:111613395..111642090hg19UCSC Ensembl
InnerchrX:111500051..111528746hg18UCSC Ensembl
InnerchrX:111419540..111448235hg17UCSC Ensembl
CytobandXq23
Allele length
AssemblyAllele length
hg3828696
hg1928696
hg1828696
hg1728696
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516845
Supporting Variants
Samples
Known GenesZCCHC16
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv698960
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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